Aging
Navigate
Research Paper|Volume 13, Issue 5|pp 7589—7607

Fecal microbiota transplantation mitigates vaginal atrophy in ovariectomized mice

Jia Huang1,2, Wanying Shan1,2, Fuxia Li1,2, Zizhuo Wang1,2, Jing Cheng1,2,3, Funian Lu1,2, Ensong Guo1,2, Rajluxmee Beejadhursing1,2, Rourou Xiao1,2, Chen Liu1,2, Bin Yang1,2, Xi Li1,2, Yu Fu1,2, Ling Xi1,2, Shixuan Wang1,2, Ding Ma1,2, Gang Chen1,2, Chaoyang Sun1,2
  • 1Cancer Biology Research Center, Key Laboratory of the Ministry of Education, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei, People’s Republic of China
  • 2Department of Gynecology and Obstetrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei, People’s Republic of China
  • 3Department of Gynecology, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei, People’s Republic of China
* Equal contribution
Received: June 24, 2020Accepted: November 10, 2020Published: February 26, 2021

Copyright: © 2021 Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Vulvovaginal atrophy (VVA) is a common menopause-related symptom affecting more than 50% of midlife and older women and cancer patients whose ovarian function are lost or damaged. Regardless of estrogen deficiency, whether other factors such as the gut microbiota play role in VVA have not been thoroughly investigated. To this end, we performed ovariectomy on 12-weeks’ old mice and follow-up at 4 weeks after ovariectomy, and observed atrophied vagina and an altered gut microbiota in ovariectomized mice.. We further performed fecal microbiota transplantation with feces from another cohort of ovary-intact fecund female mice to the ovariectomized ones, and found that the vaginal epithelial atrophy was significantly alleviated as well as the gut microbiota was pointedly changed. All these results suggest that ovarian activity has some influence on the gut microbiota, and the latter from the ovary-intact female mice can somehow make the vagina of mice deficient in ovarian function healthier maybe by up-expressing ESR1 in vaginal cells and enhancing regeneration in vagina. This kind of association between gut microbiota and vaginal health need further exploration such that it may provide an alternative treatment by modulating gut microbiota in patients suffering from VVA but may be reluctant to hormone therapy.